Friderici K, Cavanagh K T, Leipprandt J R, Traviss C E, Anson D S, Hopwood J J, Jones M Z
Department of Pathology, Michigan State University, East Lansing 48824-1314, USA.
Biochim Biophys Acta. 1995 Jun 9;1271(2-3):369-73. doi: 10.1016/0925-4439(95)00054-8.
Mucopolysaccharidosis IIID results from the deficiency of N-acetylglucosamine 6-sulfatase activity. A Nubian goat with this lysosomal storage disease has been identified. As a first step in developing this animal model for testing treatment methods, we cloned and sequenced the caprine N-acetylglucosamine 6-sulfatase cDNA coding region. Overall there is 88% nucleotide homology between the goat and human sequence and 94% homology of the deduced amino acid sequence. The human and two ruminant species differ by the presence of an imperfect trinucleotide (CCG) repeat in the ruminant signal sequence.
黏多糖贮积症IIID是由N-乙酰葡糖胺6-硫酸酯酶活性缺乏引起的。已鉴定出一只患有这种溶酶体贮积病的努比亚山羊。作为开发这种用于测试治疗方法的动物模型的第一步,我们克隆并测序了山羊N-乙酰葡糖胺6-硫酸酯酶cDNA编码区。总体而言,山羊和人类序列之间的核苷酸同源性为88%,推导的氨基酸序列同源性为94%。人类和两种反刍动物物种的区别在于反刍动物信号序列中存在一个不完全的三核苷酸(CCG)重复序列。